Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L29/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
  • C08L29/02—Homopolymers or copolymers of unsaturated alcohols
  • C08L29/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J129/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Adhesives based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Adhesives based on derivatives of such polymers
  • C09J129/02—Homopolymers or copolymers of unsaturated alcohols
  • C09J129/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
  • C03C25/10—Coating
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
  • C08L3/04—Starch derivatives, e.g. crosslinked derivatives
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J103/00—Adhesives based on starch, amylose or amylopectin or on their derivatives or degradation products
  • C09J103/04—Starch derivatives
• • D—TEXTILES; PAPER
  • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
  • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
  • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
  • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
  • D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
  • D04H1/64—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
  • C08K2003/3045—Sulfates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/38—Boron-containing compounds
  • C08K2003/387—Borates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
  • C08K3/24—Acids; Salts thereof
  • C08K3/26—Carbonates; Bicarbonates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K7/00—Use of ingredients characterised by shape
  • C08K7/02—Fibres or whiskers
  • C08K7/04—Fibres or whiskers inorganic
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K7/00—Use of ingredients characterised by shape
  • C08K7/02—Fibres or whiskers
  • C08K7/04—Fibres or whiskers inorganic
  • C08K7/14—Glass
• • E—FIXED CONSTRUCTIONS
  • E04—BUILDING
  • E04B—GENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
  • E04B1/00—Constructions in general; Structures which are not restricted either to walls, e.g. partitions, or floors or ceilings or roofs
  • E04B1/62—Insulation or other protection; Elements or use of specified material therefor
  • E04B1/74—Heat, sound or noise insulation, absorption, or reflection; Other building methods affording favourable thermal or acoustical conditions, e.g. accumulating of heat within walls
  • E04B1/88—Insulating elements for both heat and sound

Definitions

• the present invention relates to the field of mineral fiber materials comprising a binder which is free from phenol and formaldehyde, which can be used in producing fibrous, thermal, and acoustical insulation products intended for various applications.
• Mineral and rock wool is a fibrous material obtained from the melts of gabbro-basalt rocks as well as smelter slags and mixtures thereof.
• Mineral wool is a known highly efficient material for use in thermal or acoustical insulation. Melting point of the fibers exceeds 1000°C, which allows using mineral wool products in a wide range of operating temperatures. A huge number of the material advantageous properties makes it one of the most popular insulation and soundproofing materials.
• Mineral wool has unique properties such as a fire resistance, biological and chemical resistance to various aggressive substances, fungal resistance and rodent resistance. At the same time, mineral wool meets the current sanitary and hygienic standards and quality standards. In addition, mineral wool exhibits a volume and shape stability in any conditions; it has low thermal conductivity, high thermal resistance and high strength.
• Mineral fiber products generally comprise mats, boards and roll products of glass fiber, mineral wool and rock wool, where the fibers are bonded together by a cured thermoset polymeric binder material.
• the rough fibrous materials (webs, mats) used for the subsequent manufacturing of thermal and acoustic insulating products of various types using mechanical processing are generally produced by converting a melt of suitable raw materials to fibers in a conventional manner, for instance by a spinning cup process.
• the melt fibers formed in the centrifuge are blown into a fiber deposition chamber and - while airborne and while still hot - are covered by a binder solution and randomly deposited as a primary mat onto a travelling moving conveyor.
• the fiber mat is then mechanically formed from a primary mat of a desired thickness and continuously fed to a polymerization chamber where heated air is blown through the mat to cure the binder and bond the mineral fibers together.
• the resulting carpet blank (mat) is cooled off by cold-air sweeping and cut into finished products (boards) or rolled up.
• the conventional binders for mineral fibers are phenol-formaldehyde resins. Since they are relatively cheap, they have a low viscosity and are capable to cure forming a hard polymer, thereby resulting in a final product with good physical and mechanical properties.
• phenol-formaldehyde binders is becoming increasingly undesirable because of toxic chemicals (phenol and formaldehyde) that pollute the environment during their production and are emitted during their use.
• non-phenol formaldehyde binders A number of formaldehyde free compositions (so-called non-phenol formaldehyde binders) have been developed for use as binders in the production of fiber products.
• the main disadvantage of these solutions is poor workability in their application, due to the incompatibility of the proposed non-phenol-formaldehyde binders with traditional phenol-formaldehyde resin.
• long stoppages of the process equipment is required for cleaning and washing the lines when switching from the production of non-phenol-formaldehyde grades of thermal insulation products to traditional phenolic ones, which occurs in practice when using polyacrylic acid binders (which have a strongly acidic pH and are therefore poorly compatible with weakly basic phenol formaldehyde resin).
• binders according to RU 2430124 (publ. 09/27/2011), where a composition for producing a fiber nonwoven material (in particular, of synthetic fiber - polyester, acrylic, nylon, polyamide, ceramic or fiberglass) and a method of impregnating the loose mass of fibers with a solution of a binder is disclosed.
• a curable aqueous composition for a nonwoven fabric binder is obtained by a method comprising combining the following components:
• Weight ratio of components (a):(b) ranges from 95:5 to about 35:65, and a pH of the curable composition is increased to at least 1.25 by adding nitrogen containing base.
• the non-polymeric polyaldehyde is a blocked glyoxal or a blocked glutaraldehyde, which is blocked by a blocking agent, which is at least one agent selected from the group consisting of urea, ethylene urea, sorbitol and ethylene glycol.
• This method is applicable for a nonwoven fabric, but exhibits insufficient water resistance for mineral wool products. Furthermore, the use in the fiber production significant amounts of a multifunctional cross-linking chemical agent (such as maleic anhydride, glyoxal or glutaraldehyde) does not allow declaring the absolute environmental safety of such production process and the resulting fibrous thermal insulating products obtained from this fiber.
• a multifunctional cross-linking chemical agent such as maleic anhydride, glyoxal or glutaraldehyde
• a fibrous insulation product includes a binder comprising a polyol and a phosphorus crosslinking agent derived from a phosphonic or phosphoric acid, salt, ester or anhydride to form crosslinked phosphodiester linkages.
• the polyol and the crosslinking agent form a polyester thermosetting resin, more particular a phosphodiester crosslinked resin.
• the heat-insulation and sound-insulating material contains mineral fibres, binding agent and nano- or microparticles.
• Binding agent is produced by hardening aqueous composition containing polyvinyl alcohol, modified starch, crosslinking agent, catalyst, silane, dust-removing oil and water repellent.
• Nano- or microparticles are made of at least one material selected from a group comprising graphite, fullerenes, carbon nanotubes, clay, particles of metals and their alloys, carbides and oxides, silicon dioxide microparticles (microspheres) or any combination of the above objects, or any combination thereof. Nano- or microparticles are used to create a denser network of cross-linkings, resulting from interaction of polycondensation or polymerization centers, various reactive functional groups of the binder, which provides better curing of the components of the binder.
• the nano- and microparticles tendency to spontaneous agglomeration and sedimentation causes their uneven distribution in the binder, thus, there is a risk of heterogeneity of the of the resulting insulating material.
• some types of particles cause rapid, within 4-6 hours, abrasion of centrifuge nozzles due to friction, and therefore the supply of the binder to the fibers becomes unstable. In this case, the spraying uniformity of the binder is negatively affected; the binder is unevenly distributed on the fiber.
• consumption of binder is to be increased for eliminating the uneven bonding of the fibers in the products, which leads to an increase in the flammability of the finished product. Therefore, after 4 hours of work, it is necessary to stop production to replace centrifuge nozzles.
• the binder according to the patent RU 2588239 requires high drying and curing temperatures - not less than 260°C. This results in binder losses in the polymerization chamber in amount of about 30-40% on dry weight basis, caused by partial destruction of the initial components.
• the solution to the problem is reducing the curing temperature of the binder components, as well as facilitating dehydration and decreasing polycondensation temperature.
• thermal and sound insulating material that comprises mineral fibers with a diameter of 0.5 to 10.0 microns and a binder composition comprising a nontoxic polymeric component that bounds these fibers and is capable to pass to non-melting and insoluble state due to the process of its autonomous catalytic thermo dehydration, intermolecular and intramolecular crosslinking.
• the polymer component contains polyvinyl alcohol and modified starch as the main constituents and is cured from the aqueous composition.
• the binder also contains processing additives, which are common in the production of thermal and sound insulating fiber materials, such as silane, dust-removing oils, water repellent.
• the binder contains a catalytic system, which represents a combination of two different dehydrating agents. This contributes to the process of dehydration lasting the sufficient time for the carpet blank (mat) to pass through the polymerization chamber (4-10 minutes, at curing temperatures of up to 225°C). This allows to avoid the use of any additional special chemical cross-linking agents (which are involved in the intermolecular chemical reaction with hydroxyl-containing components of the binder) in the process, which ensures a significantly greater level of environmental friendliness of the products obtained.
• the catalytic system comprises two dehydrating agents - a main agent (in major amounts) and a supplemental agent (in minor amounts).
• dehydrating agents that are used for mixing are selected from the following substances:
• Distribution of the dehydrating agents in the groups is based on the fact that the main dehydrating agent is used in the process in substantially larger amounts (in the range from 0.005 wt.% to 0.02 wt.% calculated for finished product) than the supplemental dehydrating agent (in the range from 0.0007 wt.% to 0.0017 wt.%, calculated for finished product).
• the mass ratio of the main to the supplemental dehydrating agents is approximately from 7 to 29. With a larger ratio, there is an unjustified overrun of the dehydrating agent, and with a larger proportion of the supplemental dehydrating agent, the cost of the composition increases significantly without essential gain in the properties of the finished product and technological conditions.
• the combined dehydrating system which is contained in very small amounts in the finished products (no more than 0.022% by weight of the finished product) and does not pose a threat to environmental safety when used, nevertheless provides the required effect of crosslinking, functioning in a binder as a dehydration enhancer of the polyvinyl alcohol macromolecules and modified starch.
• crosslinking functioning in a binder as a dehydration enhancer of the polyvinyl alcohol macromolecules and modified starch.
• the binder film which binds together the individual fibers of the thermal-insulating material, becomes durable and water-insoluble, which provides the necessary set of strength, compressibility and water resistance consumer properties of the resulting products.
• Catalytic dehydration of polyvinyl alcohol using a variety of dehydrating agents have been known in the prior art, however, it was unexpectedly discovered that a combination of two dehydrating agents according to the invention taken in a selected proportion (the main agent in major amounts of and the supplemental agent in minor amounts) allows reducing temperature and duration of the curing process significantly. It became possible to use catalytic dehydration for a binder containing polyvinyl alcohol and modified starch as a result. This can be considered an environmentally friendly binder for mineral fibers.
• the use of a combination of the dehydrating agents allows reducing the process temperature with the same time of passing the polymerization chamber from 260° C (without supplemental dehydrating agents) or 245° C (with a single main dehydrating agent) to a range from 207° C to 225° C (when using a combination of main and supplemental dehydrating agents), which is technologically very advantageous in terms of energy savings.
• the finished material contains: 92.0 to 98.0 wt. % of the mineral fibers and 0.95 to 7.00 wt. % of the binder (including - polyvinyl alcohol in amount from 0.72 to 4.00 wt.%, modified starch in amount from 0.01 to 3.00 wt.%, and in addition - processing additives: silane, dust-removing oils, water repellent) and the combination of the dehydrating agents in amount from 0.007 to 0.02 2 wt. %
• the material After curing the binder, the material contains up to 7.0 wt% of the cured polymer, more preferably - from 0.95 to 4.3 wt% of the cured polymer.
• a method for producing a heat and sound insulating material according to claim 1 wherein the melt-formed mineral or glass fiber is fed to the centrifuge simultaneously with a phenol and formaldehyde-free binder composition containing polyvinyl alcohol, modified starch, processing additives and a combination of two dehydrating agents, wherein at least one main dehydrating agent is selected from the group comprising an organic titanium compound, organic nickel compound and a boron compound, and at least one supplemental dehydrating agent is selected from the group comprising silver salt, rhenium salt, zirconium salt and a cerium salt; thereafter the obtained carpet blank is shaped to the desired thickness and subjected to heat treatment.
• a phenol and formaldehyde-free binder composition containing polyvinyl alcohol, modified starch, processing additives and a combination of two dehydrating agents, wherein at least one main dehydrating agent is selected from the group comprising an organic titanium compound, organic nickel compound and a boron compound, and at least one supplemental dehydrating
• Processing additives include silane, dust-removing oil and water-repellent emulsion.
• the composition of the binder is mixed on the mineral wool products manufacture site immediately before it is applied to the fiber, by successively mixing all the components.
• the aqueous solutions of polyvinyl alcohol and modified starch are mixed first, then the processing additives are introduced to the solution followed by adding the combination of the dehydrating agents.
• the binder composition may be loaded with the dehydrating agents either in the solid form, or in the form of a solution or suspension in a suitable solvent.
• Heat treatment of carpet blanks of fibrous material is carried out at a temperature of 220 -230° C for a time sufficient to dry it and to complete the process of curing the binder, preferably for 4-10 minutes.
• the amount of the binder components is calculated taking into account the loss of mineral fibers during the fiber formation and the binder is fed to the centrifuge with an excess of 18%.
• the resulting carpet blanks are cut into boards, or rolled up to obtain the finished products.
• the proposed method does not require modification of the existing technology used for manufacturing the products from mineral fiber since conventional mineral fibers are used with a diameter of 0.5 to 10.0 ⁇ m, and having any suitable chemical composition - basalt, glass or slag.
• the density of the resulting fibrous material may vary from 10 to 185 kg/m 3 (preferably from 25 to 120 kg/m 3 ), which also meets the requirements for such products.
• Heat and sound insulation fibrous products of the present invention were obtained by applying a phenol and formaldehyde-free binder to a melt-formed mineral or glass (slag) fiber.
• the resulting primary mat was then formed to the desired thickness of the carpet blank (mat) fibrous material and heat treated to cure the binder composition to obtain an infusible and insoluble polymer which binds individual fibers together forming a solid fibrous product.
• Heat treatment of carpet blanks (mat) of fibrous material is performed at an average temperature of 225° C for a time sufficient to its drying and completing the binder curing process (4-10 minutes).
• the final product contains up to 7.0 wt.% of the cured polymer, more preferably from 0.95 to 4.3 wt.% of the cured polymer, wherein the weight percentages are calculated based on the amount of fiber and cured polymer.
• the carpet blank (mat) thus obtained cooled by drawing cold air and cut to the finished products (boards) or wound into the roll product.
• a solution of modified starch (component A) was prepared by dissolving 30 kg of starch or modified starch in 70 liters of demineralized water.
• a solution of polyvinyl alcohol (component B) was prepared by dissolving 30 kg of polyvinyl alcohol in 70 1 of demineralized water.
• the processing additives were added according to the formulation, and the binder thus obtained was diluted with water to a concentration of 9%, prior to feeding to the centrifuge.
• Example 1 Production of heat insulation products with an average density (35-45 kg/m 3 ).
• the resulting binder is continuously fed to the centrifuge simultaneously with the melt, to cover the fiber by the composition.
• a primary mat was formed from the fiber covered by the binder, the mat then dried and cured in a polymerization chamber at a temperature of 220-230°C, with hot air being purged through the mineral wool carpet. Then the carpet was cooled by drawing cold air there through and cut into the finished products.
• Example 2 Production of heat-insulation products with low density (25-35 kg/m 3 ).
• This Example differs from the Example 1 by the reduced load for mixing the binder components listed in table 2, namely:
• Example 3 Production of heat-insulation products with high density (more than 100 kg/m 3 ), using a combination of two dehydrating agents from the Group 2.
• Example 2 differs from the Example 1 by the increased load of the binder components listed in table 3, for mixing, namely:
• Example 4 Production of insulation products with an average density (80-90 kg/m 3 ).
• Table 4 Composition of the binder: kg per 1 ton of finished products % supply of dry residue per ton of finished products, including 18% loss % of the component per 1 ton of finished products Component A (main substance content - 30%) 47 1.42 1.2 Component B (main substance content - 30%) 47 1.42 1.2 Water 219 - Dust remover Pentamix 842 10.7 0.535 0.454 Water-repellent Silres BS 5136 10.2 0.51 0.435 Silane - Silquest A 1524 0.63 0.063 0.053 Dehydrating Agent of Group 1 Tetrabutoxytitanium 0.1 0.01 0.1 Dehydrating Agent of Group 2 Silver oxalate 0.020 0,002 0,0017 Total binder and additives 334.83 100 3,444 Mineral fiber (basalt) 96,556 Total 100
• Example 5 Production of heat-insulating products with high density (more than 100 kg/m 3 ) using the dehydrating agent from the Group 1 only, without any additional dehydrating agents from the Group 2.
• Example 6 Production of heat-insulating products made of fiberglass with a density of 11 - 46 kg/m 3 .
• This Example differs from the Examples 1-5 for the basalt fiber with a higher binder content of up to 7%.
• Binder component loading
• Example 7 Producing heat-insulating products from slag wool with a density of more than100 kg /m 3 .
• This Example differs from the Example 3 with the reduced load of component A to ensure the tactile softness of the heat-insulating boards.
• Curing the products with the compositions according to the Examples 1-4 in the polymerization chamber required a temperature of 210 to 230°C to ensure water absorbability of up to 1 kg/m 2 , and for the product according to the composition of the Example 5 without any additional dehydrating agents of group 2, the temperature of 245°C was required to provide the same water absorbability.
• Example 1 Example 2
• Example 3 Example 4
• Example 5 Example 6
• Example 7 Density, kg/m 3 38 ( ⁇ 4) 30 ( ⁇ 4) 110( ⁇ 5) 80-90 110( ⁇ 5) 14 125 Heat-transfer capacity at 25°C, W/(m ⁇ K) up to 0.039 0.039 0.038 0.038 0.038 0.042 0.039 Compressibility, %), up to 30.0 30.0 - 30 - - - Compression strength at 10% deformation, kPa, up to - - 20 - 17 - 21 Organic content, wt.%, up to 2.5 1.0 7.0 2.5 7.0 8 5.22 Water absorbability at short time and partial immersion, kg/m 2 , up to 1.0 1,0 1.0 1.0 1.0 2 1.5 Humidity, wt. %, up to 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5
• the resulting product is highly competitive with the material produced with the conventional phenol-formaldehyde resins, and/or according to the methods of producing fibrous products with the non-phenol-formaldehyde binders known in the state of the art, but the product of the present invention exhibits greater environmental safety as at the production stage, and in use.
• the present invention provides for significant improvements of the processability of the manufacturing process for the fibrous material products with a non-phenoformaldehyde binder, eliminates the drawbacks of previously used and proposed methods, in particular, allows to avoid using nano-and microparticles eliminates the need for their thorough distribution in the bulk liquid binder.
• the proposed technology retains main advantages of the conventional methods such as good compatibility with phenolformaldehyde binders (which simplifies transition from one brand of fibrous insulation products to another), and low toxicity of the main chemical components used (polyvinyl alcohol and modified starch), which allows producing the heat and sound insulation products that are more safe.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Medicinal Chemistry (AREA)
• General Life Sciences & Earth Sciences (AREA)
• Polymers & Plastics (AREA)
• Health & Medical Sciences (AREA)
• Geochemistry & Mineralogy (AREA)
• Materials Engineering (AREA)
• Dispersion Chemistry (AREA)
• Textile Engineering (AREA)
• Nonwoven Fabrics (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
• Artificial Filaments (AREA)
• Chemical Or Physical Treatment Of Fibers (AREA)

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• 2017
  • 2017-09-06 RU RU2017131349A patent/RU2688549C2/ru active
• 2018
  • 2018-10-30 WO PCT/RU2018/050133 patent/WO2019050439A2/ru not_active Ceased
  • 2018-10-30 EP EP18854731.9A patent/EP3680292A4/de not_active Withdrawn

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